IP Library Granted Patent US 10,577,397
Granted Patent B2
US 10,577,397 · App. 16/041,395 · Granted Mar 3, 2020

Methods and compositions for protein delivery

Inventors: Deb Chatterjee (Potomac, MD); Stanislaw Jan Kaczmarczyk (Frederick, MD)
Assignee: The USA, as represented by the Secretary, Dept. of Health and Human Services
C07K14/005A61K47/6901C07K14/00C07K14/245C12N7/00C07K2319/09C07K2319/10C07K2319/50C07K2319/705C07K2319/735C12N2740/13043C12N2760/20222C12N2760/20223C12N2810/6072C12N2810/6081
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Quick Facts
Patent No.
US 10,577,397
App. No.
16/041,395
Granted
Mar 3, 2020
Kind
B2
Abstract

The present invention provides methods and compositions for protein delivery. The invention features virus like particles, methods of making virus like particles and methods of using virus like particles to deliver proteins to a cell, to provide protein therapy and to treat diseases or disorders. The invention also features methods of targeting a protein to a cell, methods of protein therapy and methods of treating diseases or disorders using a TUS protein, a NLS or NES identified from full length TUS.

Claims (18)

1. A pharmaceutical composition comprising a VLP which further comprises a Gag fusion protein comprising a matrix protein, a capsid protein, a nucleocapsid protein, covalently linked to a protein of interest selected from the group consisting of a cytotoxic enzyme, an interferon, a tumor suppressor, a recombinase, a hormone, and a stem cell transcription factor; a fusogenic protein having reduced ligand-binding activity; and a nuclear localization signal (NLS) comprising at least a portion of SEQ ID NO: 1 or SEQ ID NO: 2.

2. The pharmaceutical composition of claim 1 , wherein the fusogenic protein is selected from the group consisting of: an influenza haemagglutinin, a respiratory syncytial virus fusion protein, a tick borne encephalitis virus or dengue fever virus E protein, a Semliki Forest virus E1 protein, a rabies virus or vesicular stomatitis virus (VSV) G protein, a baculovirus gp64, and fragments thereof.

3. The pharmaceutical composition of claim 1 , wherein the Gag fusion protein does not comprise a reverse transcriptase, a protease, or an integrase.

4. The pharmaceutical composition of claim 1 , further comprising a second Gag fusion protein comprising a protease.

5. The pharmaceutical composition of claim 1 , wherein the fusogenic protein is an envelope glycoprotein or fragment thereof.

6. The pharmaceutical composition of claim 5 , wherein the envelope glycoprotein is from an RNA virus or a retrovirus.

7. The pharmaceutical composition of claim 1 , wherein the fusogenic protein is a VSV-G glycoprotein comprising a substitution at the second amino acid of (phenylalanine (F)) for cysteine (C) of the mature VSV-G protein.

8. A kit comprising the pharmaceutical composition of claim 1 .

9. The kit of claim 7 , wherein the kit further comprises instructions for using the VLP to treat a disease or disorder in a subject.

10. A kit comprising an isolated nucleic acid encoding a VLP comprising: a Gag fusion protein comprising a matrix protein, a capsid protein, a nucleocapsid protein, covalently linked to a protein of interest selected from the group consisting of a cytotoxic enzyme, an interferon, a tumor suppressor, a recombinase, a hormone, and a stem cell transcription factor; a fusogenic protein having reduced ligand-binding activity; and a nuclear localization signal (NLS) comprising at least a portion of SEQ ID NO: 1 or SEQ ID NO: 2.

11. The kit of claim 10 , wherein the fusogenic protein is selected from the group consisting of: an influenza haemagglutinin, a respiratory syncytial virus fusion protein, a tick borne encephalitis virus or dengue fever virus E protein, a Semliki Forest virus E1 protein, a rabies virus or vesicular stomatitis virus (VSV) G protein, a baculovirus gp64, and fragments thereof.

12. The kit of claim 10 , wherein the Gag fusion protein does not comprise a reverse transcriptase, a protease, or an integrase.

13. The kit of claim 10 , further comprising a second Gag fusion protein comprising a protease.

14. The kit of claim 10 , wherein the fusogenic protein is an envelope glycoprotein or fragment thereof.

15. The kit of claim 14 , wherein the envelope glycoprotein is from an RNA virus or a retrovirus.

16. The kit of claim 10 , wherein the fusogenic protein is a VSV-G glycoprotein comprising a substitution at the second amino acid of (phenylalanine (F)) for cysteine (C) of the mature VSV-G protein.

17. The kit of claim 10 , wherein the kit further comprises a host cell line.

18. The kit of claim 17 , wherein the kit further comprises instructions for making a VLP.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 14, 2019
From: CHATTERJEE, DEB; KACZMARCZYK, STANISLAW JAN
To: THE USA, AS REPRESENTED BY THE SECRETARY, DEPT. OF HEALTH AND HUMAN SERVICES
Reel/Frame 049176/0489 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 15, 2018
From: CHATTERJEE, DEB; KACZMARCZYK, STANISLAW JAN
To: THE USA, AS REPRESENTED BY THE SECRETARY, DEPT. OF HEALTH AND HUMAN SERVICES
Reel/Frame 047169/0123 →
Continuity (4)
Continuation 15082401 · Mar 28, 2016
Division 13122513
Provisional Application 61195084 · Oct 3, 2008
Related Publication 20190135869A1 · May 9, 2019
Cited By (4)
US 12,319,938 US 12,351,814 US 12,351,815 US 12,404,525